A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873949



Internal ID22648899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233450163..233450298hg38UCSC Ensembl
chr1:233585909..233586044hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873949
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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